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BETULA LENTA POLLEN - 0268-1070-50 - (Birch White)

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Drug Information of BETULA LENTA POLLEN

Product NDC: 0268-1070
Proprietary Name: BETULA LENTA POLLEN
Non Proprietary Name: Birch White
Active Ingredient(s): .05    g/mL & nbsp;   Birch White
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of BETULA LENTA POLLEN

Product NDC: 0268-1070
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of BETULA LENTA POLLEN

Package NDC: 0268-1070-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-1070-50)

NDC Information of BETULA LENTA POLLEN

NDC Code 0268-1070-50
Proprietary Name BETULA LENTA POLLEN
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-1070-50)
Product NDC 0268-1070
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Birch White
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name BETULA LENTA POLLEN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of BETULA LENTA POLLEN


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